GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdh in Echinicola vietnamensis KMM 6221, DSM 17526

Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate Echvi_3019 Echvi_3019 Glucose/sorbosone dehydrogenases

Query= BRENDA::I7A144
         (352 letters)



>FitnessBrowser__Cola:Echvi_3019
          Length = 387

 Score =  182 bits (461), Expect = 2e-50
 Identities = 114/332 (34%), Positives = 166/332 (50%), Gaps = 35/332 (10%)

Query: 24  EEVVGGLEVPWALAFLPDGGMLIAERPGRIRLFREGRLSTYAELP-VYHRGESGLLGLAL 82
           E +V  +  PW +A LPDGG+L+ E+ G +   ++G        P V  +G+ GLL + L
Sbjct: 52  ETIVEDINNPWGMALLPDGGILVTEKAGELIYAKDGEKKIIPGTPDVVSKGQGGLLDIIL 111

Query: 83  HPRFPEAPYVYAYRTVAEG---GLRNQVVRLRHLGERGVLDRVVLDGIPARPHGLHSGGR 139
           HP +    ++Y   +  EG   G    V+R +  G       V+    P    G H G R
Sbjct: 112 HPDYATNGWIYFTYSSGEGEEDGAHTAVMRAKFHGNSLTDQEVLYKATPNTDKGQHFGSR 171

Query: 140 IAFGPDGMLYVTTGEVYEREL-AQDLASLGGKILRLTPEGEPAPGNPFLGRRGARPEVYS 198
           +AF  +G LY + GE  ER++  QD+   GGKI R+  +G     NPF     A+  ++S
Sbjct: 172 MAFDEEGYLYFSIGERGERDVNPQDITRDGGKIYRIHDDGSIPNDNPFFNEEDAKKAIFS 231

Query: 199 LGHRNPQGLAWHPKTGELFSSEHGPSGEQGYGHDEVNLIVPGGNYGWPRVVGRG------ 252
            GHRNPQG+ +HP   E++ +EHGP      G DE+N++  GGN+GWP VV  G      
Sbjct: 232 YGHRNPQGMIFHPVYNEIWVNEHGPQ-----GGDEINIVEKGGNFGWP-VVSYGINYDDS 285

Query: 253 ------NDPRYRDPLYFW-----PQGF---PPGNLAFFRGDLYVAGLRGQALLRLVLEGE 298
                 +      PLY+W     P GF   P      + G+L V  L+ Q L  L L+G+
Sbjct: 286 ILTEETSKEGMEQPLYYWVPSIAPCGFALVPEETYPQWAGNLLVGSLKFQYLEMLSLDGK 345

Query: 299 RGRWRVLRVETALSGFGRLREVQVGPDGALYV 330
               +V +    + G GRLR V++GPD  +YV
Sbjct: 346 ----QVTKRTKLMDGAGRLRNVKIGPDNHIYV 373


Lambda     K      H
   0.322    0.146    0.460 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 498
Number of extensions: 37
Number of successful extensions: 6
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 352
Length of database: 387
Length adjustment: 30
Effective length of query: 322
Effective length of database: 357
Effective search space:   114954
Effective search space used:   114954
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory